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On study day 2, between 04:00 h and 09:00 h, a simultaneous, primed (60 the 1 min infusion rate), 5 h constant-rate infusion was initiated with [6,6- 2 H 2 ]glucose (0.09 mg kg FFM 1 min 1 ) and [ 2 H 5 ]glycerol (0.015 mg kg FFM 1 min 1 ) to measure glucose and glycerol turnover, respectively

New Drug Application (NDA): If clinical trials demonstrate that the drug is safe and effective, the sponsor submits an NDA to the FDA, which includes all data from the trials, labeling information, and manufacturing details
